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日本厚生劳动省难治性血管炎研究委员会关于显微镜下多血管炎和肉芽肿性多血管炎管理的临床实践指南:2023年更新——二次发表

Clinical practice guidelines of the Japan Research Committee of the Ministry of Health, Labour, and Welfare for Intractable Vasculitis for the management of microscopic polyangiitis and granulomatosis with polyangiitis: The 2023 update - secondary publication.

作者信息

Sada Ken-Ei, Nagasaka Kenji, Kaname Shinya, Nango Eishu, Kishibe Kan, Dobashi Hiroaki, Hiromura Keiju, Kawakami Tamihiro, Bando Masashi, Wada Takashi, Amano Koichi, Murakawa Yohko, Harigai Masayoshi

机构信息

Department of Rheumatology, Ome Municipal General Hospital, Ome, Japan.

Department of Rheumatology, Tokyo Medical and Dental University (TMDU), Tokyo, Japan.

出版信息

Mod Rheumatol. 2024 Mar 28;34(3):559-567. doi: 10.1093/mr/road081.

Abstract

OBJECTIVE

To revise the 2017 clinical practice guidelines (CPG) for the management of microscopic polyangiitis (MPA) and granulomatosis with polyangiitis (GPA) to reflect advancements in the field.

METHODS

Similar to the 2017 CPG, the Grading of Recommendations, Assessment, Development, and Evaluation system was adopted for this revision. The intended users of this CPG include patients diagnosed with MPA or GPA in Japan and their families and healthcare professionals, including specialists and non-specialists. Based on a scoping review, four clinical questions (CQs) of the 2017 guidelines were modified, and six new CQs were added.

RESULTS

We suggest a combination of glucocorticoid and cyclophosphamide or rituximab for remission induction therapy. In cases where cyclophosphamide or rituximab is used, we suggest the use of avacopan over high-dose glucocorticoid. Furthermore, we suggest against the use of plasma exchange in addition to the standard treatment in severe cases of MPA/GPA. Finally, we suggest the use of glucocorticoid and rituximab over glucocorticoid and azathioprine for remission maintenance therapy.

CONCLUSIONS

The recommendations have been updated based on patient preference, certainty of evidence, benefit and risk balance, and cost.

摘要

目的

修订2017年显微镜下多血管炎(MPA)和肉芽肿性多血管炎(GPA)管理的临床实践指南(CPG),以反映该领域的进展。

方法

与2017年CPG类似,本次修订采用了推荐分级、评估、制定和评价系统。本CPG的目标用户包括在日本被诊断为MPA或GPA的患者及其家属以及医疗保健专业人员,包括专科医生和非专科医生。基于范围审查,对2017年指南的四个临床问题(CQs)进行了修改,并新增了六个CQs。

结果

我们建议糖皮质激素联合环磷酰胺或利妥昔单抗用于诱导缓解治疗。在使用环磷酰胺或利妥昔单抗的情况下,我们建议使用阿伐可泮而非高剂量糖皮质激素。此外,我们不建议在MPA/GPA重症病例的标准治疗基础上再加用血浆置换。最后,我们建议糖皮质激素联合利妥昔单抗用于维持缓解治疗,而非糖皮质激素联合硫唑嘌呤。

结论

这些建议已根据患者偏好[此处原文有误,应为preference]、证据确定性、获益与风险平衡以及成本进行了更新。

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